Wakade A R, Wakade T D, Kulkarni J S
Department of Pharmacology, Wayne State University School of Medicine, Detroit, MI 48201, USA.
Neurosci Lett. 1998 Aug 21;252(3):163-6. doi: 10.1016/s0304-3940(98)00553-9.
Our past work on nucleoside toxicity in sympathetic neurons has clearly revealed that adenosine and 2'-deoxyadenosine (dAdo) have different mechanisms of action in inducing apoptotic death. For example, adenosine is toxic to neurons only during early phase of growth whereas dAdo kills even mature neurons. In this study, we hypothesize that dAdo-induced apoptosis is initiated when ATP concentration of sympathetic neurons decreases below a critical level. To prove our hypothesis we used adenosine as a tool to replenish ATP levels of sympathetic neurons. We demonstrate that dAdo toxicity in mature sympathetic neurons was fully prevented by adenosine treatment. Furthermore, we demonstrate that depletion of ATP caused by dAdo was prevented by pretreatment with adenosine. These data suggest that intracellular accumulation of adenosine could play a neuroprotective role in preventing death associated with reduction in neuronal ATP concentration.
我们过去关于交感神经元中核苷毒性的研究清楚地表明,腺苷和2'-脱氧腺苷(dAdo)在诱导凋亡性死亡方面具有不同的作用机制。例如,腺苷仅在生长早期对神经元有毒性,而dAdo甚至能杀死成熟神经元。在本研究中,我们假设当交感神经元的ATP浓度降至临界水平以下时,dAdo诱导的凋亡开始。为了验证我们的假设,我们使用腺苷作为补充交感神经元ATP水平的工具。我们证明,腺苷处理可完全预防成熟交感神经元中的dAdo毒性。此外,我们证明,腺苷预处理可预防dAdo引起的ATP耗竭。这些数据表明,腺苷在细胞内的积累可能在预防与神经元ATP浓度降低相关的死亡中发挥神经保护作用。